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MabionCD20® Compared to MabThera® and Rituxan® in Patients With Rheumatoid Arthritis (MABRIDGE)

M

Mabion

Status and phase

Withdrawn
Phase 3

Conditions

Rheumatoid Arthritis

Treatments

Biological: MabionCD20 (candidate biosimilar to rituximab)
Biological: Rituxan®
Biological: MabThera®

Study type

Interventional

Funder types

Industry

Identifiers

NCT04680962
MabionCD20-003RA

Details and patient eligibility

About

Primary objective of the study is to establish a 3-way PK similarity bridge between MabionCD20 (candidate biosimilar to rituximab), MabThera® (EU-sourced rituximab) and Rituxan® (US-sourced rituximab) following the administration of these drugs to patients with moderate-to-severe rheumatoid arthritis. Main secondary objective is to confirm therapeutic similarity between MabionCD20 and the reference rituximab.

Full description

Patients with active moderate-to-severe rheumatoid arthritis diagnosed according to the 2010 ACR criteria will be randomized to receive a blinded treatment course of either MabionCD20, EU-Rituximab (MabThera®) or US-Rituximab (Rituxan®) on the top of a stable methotrexate therapy. Two infusions of investigational drug at a dose of 1000 mg will be given at Day 1 and 15. Patients will be then followed for a minimum of 24 weeks to establish PK and therapeutic similarity and to compare PD, safety and immunogenicity parameters between the three rituximab products (Main Phase). Patients may receive a second course of investigational therapy at Week 24, provided that they meet re-treatment eligibility criteria specified in the study protocol. Subjects in MabionCD20 and EU-Rituximab groups will be continued on their assigned treatments, while all subjects in US-Rituximab group will be switched to MabionCD20. All subjects (re-treated and not re-treated) will continue the follow-up until Week 48 to collect long-term safety, immunogenicity and efficacy data.

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Male or female, age 18 - 80 years

  2. Body Surface Area (BSA) between 1.5 and 2.2 m2

  3. Confirmed diagnosis of RA diagnosed according to the revised (2010) ACR/EULAR classification criteria, with a disease duration minimum of 6 months prior to the Screening Visit

  4. Currently moderate to severe RA despite ongoing administration of an adequate MTX regimen. Moderate to severe disease is defined here as the presence of the following two criteria:

    1. Six or more swollen joints and ≥6 tender/painful joints, verified by a physician during the screening and re-confirmed at baseline visit (Day 1)
    2. DAS28 score ≥3.2 at screening
  5. No history of treatment with TNF-α inhibitor (innovative or biosimilar, authorized or investigational) at any time before the screening i.e. TNF-α inhibitor naive population.

  6. Receiving MTX treatment at a dosage of 7.5-25 mg/week for at least 12 weeks prior to screening, with the last 4 weeks at a stable dose, and willing to remain at this dose for the entire study duration

  7. Male or WOCBP must consent to use highly effective contraception, from the Screening Visit, during the intervention period, and for at least 12 months after the last dose of study intervention

  8. Female participants must not be pregnant or lactating (negative baseline serum test)

Exclusion criteria

  1. History of or current inflammatory joint disease other than RA

  2. History of or current systemic autoimmune disorder

  3. ACR functional class IV disease

  4. History of psychiatric disorder that would interfere with normal participation in the study

  5. Evidence of HBV, HCV, HIV infection

  6. Evidence of laboratory-confirmed or clinically suspected SARS-CoV-2 infection within 14 days before the study drug administration and a documented positive RT-PCR test within 72 hours before the first infusion or positive antigen test within 24 hours before the first infusion.

  7. Serious and/or uncontrolled coexisting diseases which are recognized as major contraindications to the administration of rituximab, methotrexate or any of the pre-medication components or as important risk factors for the development of severe or life-threatening SARS-CoV-2 infection or other factors, which in the Investigator's opinion, would preclude patients participation. This category includes severe pulmonary, cardiovascular, neurologic, renal and hepatic diseases, severe and inadequately controlled type 1 or 2 diabetes.

  8. Recent history or current evidence of bacterial, viral or fungal infection (excluding infections of nailbeds)

  9. History of or current active tuberculosis, with typical symptoms of M. tuberculosis infection confirmed by positive results of TB screening test or documented diagnosis prior to screening

  10. Latent tuberculosis, as documented in subject's medical records or shown by a positive or indeterminate QuantiFERON test performed at screening, in absence of typical symptoms of tuberculosis. However, a patient with latent tuberculosis may become eligible for the study if he/she meets the following criteria:

    1. Patient completed a standard TB prophylaxis prior to the screening and had no active TB or contact with active TB case after completion of the most recent prophylactic regimen OR received at least four weeks of standard TB prophylactic regimen prior to the screening visit and is capable and willing to continue on this regimen while participating in the study.
    2. Patient has no active TB at the time of screening, which must be confirmed through referral to a TB specialist if > 1 year has passed since the completion of the last prophylaxis or if the prophylaxis is still being received by the time of screening
    3. Patient had no positive findings on chest X-ray examination at screening and within three months prior to screening
  11. History of cancer (solid tumors, hematologic malignancies and other) within 5 years of the screening

  12. History of significant cytopenia or other disorder of the hematopoietic system

  13. Primary or secondary immunodeficiency

  14. Any other condition that is listed as a contraindication to receive rituximab or methotrexate therapy

  15. Recent use of biologic DMARDs or non-biologic DMARDs other than MTX within the washout periods specified in the study protocol

  16. Treatment with any of the authorized or investigational TNF-α inhibitors at any time before the screening (regardless if innovative or biosimilar).

  17. History of prior treatment with a B cell modulating or B cell depleting therapy such as, but not limited to, rituximab or other anti CD20 mAb (ocrelizumab, ofatumumab, obinutuzumab), belimumab, atacicept, tabalumab, epratuzumab and other experimental treatments

  18. Use of systemic glucocorticoids at a dose higher than 10 mg prednisolone daily or equivalent, within 2 weeks prior to Screening or between screening and Day 1

  19. Use of intraarticular hyaluronic acid injection within 28 days before the screening or between screening and Day 1.

  20. Use of any drug that has not received regulatory approval for any indication within 4 weeks or a minimum of 5 half-lives, whichever is longer, prior to the Screening Visit or planned receipt of unauthorized drug or vaccine during the study.

  21. History of prior allergic or anaphylactic reaction to rituximab therapy (or to any excipient contained in the study IMP)

  22. Serious abnormal laboratory findings, specifically:

    1. White blood cell count <3,000/μL OR neutrophil count <1,500/μL.
    2. Platelet count <75,000/μL.
    3. Aspartate aminotransferase or alanine aminotransferase >2.5 times ULN.
    4. Hemoglobin <8.0 g/dL.
    5. IgG below 5.0 mg/mL or IgM below 0.4 mg/mL.
    6. Any other clinically significant laboratory abnormality.
  23. Intolerance or contraindications to administration of MTX therapy, i.v. glucocorticoids, or to any other component of the premedication

  24. Major surgery (including joint surgery) within 8 weeks prior to Screening or planned surgery within 12 months after baseline

  25. Recent vaccination with inactivated/non-live vaccine (<4 weeks prior to study intervention infusion on Day 1) or live vaccine (<6 weeks prior to study intervention infusion on Day 1) vaccine

  26. Planned vaccination with live vaccine during the follow-up.

  27. Chronic intake of narcotic analgesics (e.g. morphine, fentanyl, hydrocodone, oxycodone, codeine).

  28. Participation in a clinical study during the 2 months prior to enrolment in the study (exemption - previously failed screening procedures in MabionCD20-003RA study).

  29. Female patients breastfeeding, pregnant or planning of pregnancy within 12 months after the last infusion of the study intervention.

  30. Blood donation or other blook loss of more than 500 ml within the last two months prior to Screening Visit.

  31. Lack of peripheral venous access.

  32. History of drug, alcohol or chemical abuse within 2 years prior to screening.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

0 participants in 3 patient groups

MabionCD20 / MabionCD20
Experimental group
Description:
Patients receive one or two treatment courses of MabionCD20, each consisting of two 1000 mg i.v. infusions at an interval of 14 days. Investigational drug will be administered at Day 1 and Day 15, and, if patient is eligible for re-treatment, also at Week 24 and Week 26.
Treatment:
Biological: MabionCD20 (candidate biosimilar to rituximab)
EU-Rituximab / EU-Rituximab
Active Comparator group
Description:
Patients receive one or two treatment courses of MabThera®, each consisting of two 1000 mg i.v. infusions at an interval of 14 days. Investigational drug will be administered at Day 1 and Day 15, and, if patient is eligible for re-treatment, also at Week 24 and Week 26.
Treatment:
Biological: MabThera®
US-Rituximab / MabionCD20
Active Comparator group
Description:
Patients receive a single treatment course of Rituxan®, consisting of two 1000 mg i.v. infusions at Day 1 and Day 15. After 24 weeks of follow-up, all patients eligible for re-treatment, are switched to receive a single treatment course of MabionCD20, consisting of two 1000 mg i.v. infusions at Week 24 and Week 26.
Treatment:
Biological: Rituxan®
Biological: MabionCD20 (candidate biosimilar to rituximab)

Trial contacts and locations

0

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Central trial contact

Bartłomiej Czubek; Adam Tuszyner

Data sourced from clinicaltrials.gov

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